首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Abnormal humoral immune responses in peripheral blood lymphocyte cultures of bone marrow transplant recipients.
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Abnormal humoral immune responses in peripheral blood lymphocyte cultures of bone marrow transplant recipients.

机译:骨髓移植受者外周血淋巴细胞培养物中异常的体液免疫反应。

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摘要

The present study was aimed at investigating recovery of humoral immunity in vitro after bone marrow transplantation in patients with acute leukemia and severe aplastic anemia. Hemolytic plaque assays were utilized to quantitate pokeweed mitogen-stimulated polyclonal immunoglobulin production and sheep erythrocyte antigen-specific antibody responses in cultures of peripheral blood mononuclear cells of 39 patients beginning at 1 month, for variable periods up to a maximum of 4 years after marrow transplantation. Three phases were identified: an early period of primary B cell dysfunction with concomitant immunoregulatory T cell abnormalities--i.e., decreased helper and increased suppressor activities; an intermediate phase in which B cell dysfunction could be attributed in large measure to immunoregulatory T cell abnormalities; and a late phase of normal B and T lymphocyte functions. Patients with graft-versus-host disease differed from those without it in that they often did not manifest increased T cell suppressor activity in the early period, and they were noted to have prolonged and profound B and T cell abnormalities in the chronic phase of their disease. In selected patients, simultaneous assessment of ratios of Leu-2 to Leu-3 antigens on T cells by monoclonal antibodies and of immunoregulatory T cell functions revealed a correlation between the two only late in the post-transplant period. These studies provide an insight into the ontogeny of B cell function in the post-transplant period and indicate that in certain situations phenotypic alterations in T cell subsets cannot reliably be used to predict abnormalities in their function in recipients of marrow transplantation.
机译:本研究旨在研究急性白血病和严重再生障碍性贫血患者骨髓移植后体外体液免疫的恢复。从39例患者的外周血单核细胞培养开始,从1个月开始的可变溶血斑测定法用于定量商陆有丝分裂原促分裂原刺激的多克隆免疫球蛋白的产生和绵羊红细胞抗原特异性抗体反应,直至骨髓移植后最多4年。确定了三个阶段:早期的原发性B细胞功能障碍,并伴有免疫调节性T细胞异常-即,辅助细胞减少和抑制活性增加;中间阶段,其中B细胞功能障碍可很大程度上归因于免疫调节性T细胞异常;以及正常的B和T淋巴细胞功能的晚期。移植物抗宿主病患者与没有移植物抗宿主病的患者的不同之处在于,他们通常在早期并没有表现出增强的T细胞抑制活性,并且被注意到在他们的慢性期中,B和T细胞异常长期且严重疾病。在选定的患者中,通过单克隆抗体同时评估T细胞上Leu-2与Leu-3抗原的比率以及免疫调节性T细胞功能,发现两者仅在移植后后期才相关。这些研究提供了对移植后B细胞功能的个体发育的见解,并表明在某些情况下,T细胞亚群的表型改变不能可靠地用于预测骨髓移植受体的功能异常。

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